نتایج جستجو برای: embolia cutis medicamentosa

تعداد نتایج: 2813  

Journal: :Annals of dermatology 2008
Hyun Chang Ko Seung Wook Jwa Margaret Song Moon Bum Kim Kyung Sool Kwon

In 2005, Kreidstein first proposed the term "Cutis pleonasmus," a Greek term meaning "redundancy," which refers to the excessive skin that remains after massive weight loss. Cutis pleonasmus is clearly distinguishable from other diseases showing increased laxity of the skin, such as pseudoxanthoma elasticum, congenital and acquired generalized cutis laxa. Although individuals who are severely o...

2017
Ariana Kariminejad Fariba Afroozan Bita Bozorgmehr Alireza Ghanadan Susan Akbaroghli Hamid Reza Khorram Khorshid Faezeh Mojahedi Aria Setoodeh Abigail Loh Yu Xuan Tan Nathalie Escande-Beillard Fransiska Malfait Bruno Reversade Thatjana Gardeitchik Eva Morava

Cutis laxa is a heterogeneous condition characterized by redundant, sagging, inelastic, and wrinkled skin. The inherited forms of this disease are rare and can have autosomal dominant, autosomal recessive, or X-linked inheritance. Three of the autosomal recessive cutis laxa syndromes, namely cutis laxa IIA (ARCL2A), cutis laxa IIB (ARCL2B), and geroderma osteodysplastica (GO), have very similar...

Journal: :Anales del Sistema Sanitario de Navarra 2008

2015
Selma Aktas Canan Turkyilmaz Sezin Unal Ebru Ergenekon

Iatrogenic calcinosis cutis presents with similar symptoms and signs of soft tissue, joint and bone infections. We present here a preterm infant with iatrogenic calcinosis cutis misdiagnosed as septhic arthritis and osteomyelitis. We hope that our case report helps to raise clinicians’awareness of this rare situation. .When swelling and erythema of extremities occur in a newborn infant after in...

Journal: :Journal of the College of Physicians and Surgeons--Pakistan : JCPSP 2014
Nadia Iftikhar Faisal Iftikhar Ahmad Ghumman Shahbaz A Janjua Amer Ejaz Umar Aftab Butt

A new-born male baby with typical features of Adams-Oliver syndrome (AOS) is described. Adams-Oliver syndrome is the association of aplasia cutis congenita with terminal transverse limb reduction defects with or without cutis marmorata telangiectatica congenita. The patient presented with brachydactyly involving all the digits of his hands and shortening of both big toes along with aplasia cuti...

Journal: :iranian journal of radiology 0
mehdi alehossein advanced diagnostic and interventional radiology research center, tehran university of medical sciences, tehran, iran masoud pourgholami department of radiology, tehran university of medical sciences, tehran, iran kamyar kamrani department of pediatrics, tehran university of medical sciences, tehran, iran mohammad soltani department of radiology, tehran university of medical sciences, tehran, iran afshin yazdi department of radiology, tehran university of medical sciences, tehran, iran payman salamati advanced diagnostic and interventional radiology research center, tehran university of medical sciences, tehran, iran; advanced diagnostic and interventional radiology research center (adir), medical imaging center, imam khomeini hospital, tehran, iran. tel: +98-2166581579, fax: +98-2166581580

cutis laxa (cl) is a rare congenital and acquired disorder characterized by loose and redundant skin with reduced elasticity. three types of congenital cutis laxa have been recognized. other findings are pulmonary emphysema, bronchiectasia, hernia and diverticulosis. we describe a female neonate involved by cutis laxa syndrome and a positive family history. we focus on the radiologic findings o...

Journal: :Turk patoloji dergisi 2015
Monisha Choudhury Kiran Agarwal Smita Singh Savita Agarwal

We report a case of idiopathic calcinosis cutis diagnosed by fine needle aspiration cytology in a 50-yr-old female who presented with a subcutaneous swelling near the left iliac crest. Cytological finding of amorphous calcium salts with histiocytes and the appropriate clinical background led to the cytodiagnosis of idiopathic calcinosis cutis as subsequently confirmed on histopathology. Pitfall...

Journal: :Journal of Investigative Dermatology 2015

Journal: :Brazilian Journal of Development 2020

Journal: :Human molecular genetics 2002
Bart Loeys Lionel Van Maldergem Geert Mortier Paul Coucke Sabine Gerniers Jean-Marie Naeyaert Anne De Paepe

Hereditary cutis laxa comprises a heterogeneous group of connective tissue disorders characterized by loose skin and variable systemic involvement. Autosomal dominant and recessive as well as X-linked forms have been described. Some dominant forms are caused by mutations in the elastine gene (ELN). The X-linked form is now classified in the group of copper transport diseases. The genetic defect...

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